Otc - Active Ingredient
iodine
Colloidal Iodineinjection
FDA Label NDC 69164-0001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Jci Colloidal Iodine Laboratory Co., Ltd. for the product Colloidal Iodineinjection (NDC 69164-0001). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding otc - active ingredient, inactive ingredient, otc - purpose, otc - keep out of reach of children, indications & usage, warnings, dosage & administration, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Inactive Ingredient
potassium iodide, hydrogen water
Otc - Purpose
disinfection effect
Otc - Keep Out Of Reach Of Children
keep out of reach of the children
Indications & Usage
Consult a physician before use
Warnings
For subcutaneous use only
keep in a room temperature
keep out of the direct sunlight
Dosage & Administration
for subcutaneous use only
Package Label.Principal Display Panel
Label (Label)
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